US10093961B2ActiveUtilityA1

Methods for diagnosis of and predicting treatment efficacy of hormone receptor expressing tumors, cancers and neoplasias

Assignee: LEUSCHNER CAROLAPriority: Dec 22, 2009Filed: Dec 21, 2010Granted: Oct 9, 2018
Est. expiryDec 22, 2029(~3.4 yrs left)· nominal 20-yr term from priority
G01N 33/575G01N 33/5758G01N 33/57515G01N 33/57545C12Q 1/68G01N 33/574G01N 33/53G01N 33/566G01N 33/76G01N 33/743G01N 33/74C07K 16/2869G01N 2800/52A61K 38/24
54
PatentIndex Score
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Cited by
20
References
5
Claims

Abstract

The invention relates to diagnosis, detection, screening, identifying and predicting methods. In various embodiments, methods of the invention include diagnosis, detection, or screening for a hyperproliferative disorder (e.g., a tumor, cancer or neoplasia) in the subject; identifying a subject that will or is likely to respond to a therapy for a hyperproliferative disorder (e.g., a tumor, cancer or neoplasia); and predicting therapeutic efficacy of a hyperproliferative disorder (e.g., a tumor, cancer or neoplasia) treatment in a subject.

Claims

exact text as granted — not AI-modified
What is claimed: 
     
       1. A method of analyzing a prostate, ovarian, breast or endometrial sample, the method comprising:
 (a) contacting the prostate, ovarian, breast or endometrial sample from a subject, with a hormone polypeptide or hormone polypeptide analog that binds to LHRH- or hCG/LH receptors under conditions allowing the hormone or hormone analog to bind the LHRH- or hCG/LH receptors; 
 (b) determining an amount of LHRH- or hCG/LH receptors in the sample by detecting the amount of hormone polypeptide or hormone polypeptide analog that is bound to the LHRH- or hCG/LH receptors in the sample; 
 (c) contacting cells obtained from the sample with a peptide comprising the cytotoxic sequence KFAKFAKKFAKFAKKFAKQHWSYGLRPG (SEQ ID NO: 1); and 
 (d) after the contacting of (c), determining the IC 50  value according to a sensitivity of the cells to SEQ ID NO:1, wherein the IC 50  value is 5.5 μM or less and wherein greater LHRH- or hCG/LH receptor expression indicates increased sensitivity of the cells. 
 
     
     
       2. The method of  claim 1 , comprising identifying a sample according to the determining of (b), wherein greater than 50% of the cells express LHRH- or hCG/LH receptors. 
     
     
       3. The method of  claim 1 , wherein the cytotoxic sequence is biotin-conjugated. 
     
     
       4. The method of  claim 1 , wherein the hormone polypeptide or hormone polypeptide analog comprises one or more D-amino acids. 
     
     
       5. The method of  claim 1 , wherein the hormone polypeptide or hormone polypeptide analog is biotin-conjugated.

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